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The Hair660™ light therapy device effectively and safely improves hair density in people with androgenetic alopecia.

Lgr6+ cells are important for tissue repair and could be a target for treating cancer and other diseases.

Omega-6 fats in certain cells boost male hormone production.

Early recognition and a team approach are crucial for managing diffuse alveolar hemorrhage in antiphospholipid syndrome.

An extremely low-birthweight infant had a rare genetic skin disease and died despite treatment.

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

A woman's severe hirsutism was caused by Leydig cell tumors in her ovaries, which improved after surgery.

Skin issues from chronic graft-versus-host disease greatly affect daily life, needing teamwork between blood and skin doctors.

People with lichen planus are more likely to have dyslipidemia, especially higher triglyceride levels.

Harlequin ichthyosis involves abnormal skin cell structures and giant mitochondria, affecting skin and hair.

Vitamin D-dependent rickets Type II causes bone problems and hair loss, and doesn't improve with Vitamin D treatment.

Dermoscopy is useful for diagnosing and monitoring discoid lupus erythematosus by showing specific skin patterns.

Scientists developed a new way to study mutations in a skin condition using blood cells, which may help diagnose and treat the disease.

THA is a rare condition with no significant clinical consequences if thyroid function is normal.

Men with Addison disease should be screened for X-linked adrenoleukodystrophy if they have hair loss.

Lichen planopilaris causes permanent hair loss and scarring due to damage to hair follicles and can be mistaken for other hair loss conditions.

MFN2 mutations cause mitochondrial problems, unusual fat distribution, and low leptin despite high body fat.

Deleting a specific protein in skin cells disrupts normal hair growth and development.

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

Removing HIF-P4H-2 from certain skin cells in mice causes hair loss on the body but not the head.

Epidermolysis bullosa in calves was not caused by mutations in the keratin genes bKRT5 and bKRT14.

AMH levels can't reliably tell the difference between LOCAH and all types of PCOS in women with excessive hair growth.

Adalimumab significantly improved Hidradenitis Suppurativa and quality of life in two patients.

A protein called HMGB1 helps hair grow by affecting prostaglandin metabolism.

Mutations in the LSS gene cause hair loss and may affect brain development, with varying severity.

One twin girl has Loose anagen syndrome with poorly anchored hair, diagnosed with a simple hair pull test, while her identical twin does not have the condition.

Mutations in Plcd1 and Plcd3 together cause severe hair loss in mice.

JAK inhibitors can be safely used in alopecia areata patients with latent hepatitis B or tuberculosis, with proper monitoring.

A woman's liver problems improved after she stopped taking spironolactone.

The DWLSM provides detailed imaging of hair shafts and follicles with high accuracy.